
CAS 163931-61-1: Tetrabutylammonium triphenyldifluorosilicate (TBAT)
Formula:C34H51F2NSi
InChI:InChI=1/C18H15F2Si.C16H36N/c19-21(20,16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18;1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4/h1-15H;5-16H2,1-4H3/q-1;+1
SMILES:c1ccc(cc1)[Si-](c1ccccc1)(c1ccccc1)(F)F.CCCCN(CCCC)(CCCC)CCCC
Synonyms:- Tetrabutylammonium triphenyldifluorosilicate
- Tbat
- Tetrabutylammonium difluorotriphenylsilicate
- N,N,N-tributylbutan-1-aminium difluoro(triphenyl)silicate(1-)
- Tetrabutylamoniumdifluorotriphenylsilicate
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Found 4 products.
Tetrabutylammonium Difluorotriphenylsilicate
CAS:Controlled ProductStability Moisture Sensitive Applications Tetrabutylammonium Difluorotriphenylsilicate is used as a reagent in the synthesis of (S)-N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-fluoropropyl)-6-methoxypyridin-2-amine ((-)-P7C3-S243); a neuroprotective chemical with improved druglike properties. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Naidoo, J., et al.: J. Med. Chem., 57, 3754 (2014)Formula:C18H15F2Si·C16H36NColor and Shape:NeatMolecular weight:539.858Tetrabutylammonium Difluorotriphenylsilicate
CAS:Formula:C34H51F2NSiPurity:>97.0%(T)(qNMR)Color and Shape:White to Almost white powder to crystalMolecular weight:539.87Tetrabutylammonium difluorotriphenylsilicate
CAS:Tetrabutylammonium difluorotriphenylsilicatePurity:98%Molecular weight:539.86g/molTetrabutylammonium difluorotriphenylsilicate
CAS:Tetrabutylammonium difluorotriphenylsilicate is a model system for studying the mechanism of nucleophilic substitution at an unsymmetrical carbon center. It is used in analytical chemistry to prepare samples for analysis. Tetrabutylammonium difluorotriphenylsilicate has been shown to be an effective and selective reagent for the synthesis of picolinic acid, which can be used as a precursor for the synthesis of nicotinamide riboside, a vitamin B3 derivative. The reaction proceeds via an SN2 mechanism, where hydrogen fluoride (HF) acts as a nucleophile that attacks the electrophilic carbon center of allyl chloride (CH2=CH-CH2Cl) to form an intermediate with two alkyl groups on opposite sides. The reaction product is then hydrolyzed to release tetrabutylammonium chloride (tBuNH4Cl).Formula:C34H51F2NSiPurity:Min. 95%Color and Shape:White PowderMolecular weight:539.86 g/mol